U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 296

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144123insertion1nstd232human GRCh37.p13 chr9: 32,420,098-32,420,098 , GRCh38.p12 chr9: 32,420,100-32,420,100 ACO1
    nsv7098455copy number variation6nstd102humanUncertain significance GRCh37 chr9: 32,453,279-37,785,041 , GRCh38.p12 chr9: 32,453,281-37,785,044 TRBVAOR9-2, UBAP2, 197 more genes
    nsv7098080copy number variation1nstd102humanUncertain significance GRCh37 chr9: 32,453,279-35,068,379 , GRCh38.p12 chr9: 32,453,281-35,068,382 SUGT1P1, RNU7-36P, 110 more genes
    nsv7063062inversion1nstd229human GRCh38 chr9: 22,592,329-32,576,343 , GRCh37.p13 chr9: 22,592,328-32,576,341 HSPA8P17, RMRPP5, 81 more genes
    nsv7060710inversion1nstd229human GRCh38 chr9: 32,390,061-32,390,245 , GRCh37.p13 chr9: 32,390,059-32,390,243 ACO1
    nsv7058737inversion1nstd229human GRCh38 chr9: 32,383,965-32,384,007 , GRCh37.p13 chr9: 32,383,963-32,384,005 ACO1
    nsv6877731copy number variation1nstd229human GRCh38 chr9: 32,412,096-32,415,291 , GRCh37.p13 chr9: 32,412,094-32,415,289 ACO1
    nsv6872931copy number variation1nstd229human GRCh38 chr9: 29,015,647-32,650,007 , GRCh37.p13 chr9: 29,015,645-32,650,005 NDUFB6, LOC105376011, 32 more genes
    nsv6871194copy number variation1nstd229human GRCh38 chr9: 32,421,473-32,421,821 , GRCh37.p13 chr9: 32,421,471-32,421,819 ACO1
    nsv6863522copy number variation1nstd229human GRCh38 chr9: 32,446,917-32,447,061 , GRCh37.p13 chr9: 32,446,915-32,447,059 ACO1
    nsv6861072copy number variation1nstd229human GRCh38 chr9: 32,420,093-32,420,177 , GRCh37.p13 chr9: 32,420,091-32,420,175 ACO1
    nsv6860825copy number variation1nstd229human GRCh38 chr9: 32,434,537-32,457,315 , GRCh37.p13 chr9: 32,434,535-32,457,313 RIGI, ACO1
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6634409copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 1-40,036,525 , GRCh38.p12 chr9: 10,001-39,445,729 ACO1, PLIN2, 594 more genes
    nsv6453110copy number variation1nstd223human GRCh38 chr9: 32,382,401-32,390,300 , GRCh37.p13 chr9: 32,382,399-32,390,298 ACO1
    nsv6441694copy number variation1nstd223human GRCh38 chr9: 32,322,887-32,391,644 , GRCh37.p13 chr9: 32,322,885-32,391,642 ACO1, LOC107987059, 1 more genes
    nsv6315463copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-35,903,398 , GRCh38.p12 chr9: 203,861-35,903,401 IFNA11P, RNU6-14P, 495 more genes
    nsv6315415copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-68,342,786 , GRCh38.p12 chr9: 203,861-67,920,552 LOC107987068, FAM74A7, 846 more genes
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6314243complex chromosomal rearrangement41nstd102humanPathogenic GRCh37 chr2: 167,032,703-167,032,703 , GRCh37 chr2: 167,393,746-167,393,746 , GRCh37 chr2: 167,393,746-167,393,746 , GRCh37 chr2: 167,404,982-167,404,982 , GRCh37 chr2: 174,873,171-174,873,171 , GRCh37 chr2: 175,479,069-175,479,069 , GRCh37 chr2: 175,479,070-175,479,070 , GRCh37 chr2: 176,643,949-176,643,949 , GRCh37 chr2: 180,737,216-180,737,216 , GRCh37 chr2: 181,096,224-181,096,224 , GRCh37 chr2: 181,414,520-181,414,520 , GRCh37 chr7: 149,006,954-149,006,954 , GRCh37 chr8: 57,149,801-57,149,801 , GRCh37 chr8: 58,550,183-58,550,183 , GRCh37 chr8: 58,906,790-58,906,790 , GRCh37 chr8: 59,535,602-59,535,602 , GRCh37 chr9: 13,643,427-13,643,427 , GRCh37 chr9: 14,497,726-14,497,726 , GRCh37 chr9: 15,353,188-15,353,188 , GRCh37 chr9: 30,570,813-30,570,813 , GRCh37 chr9: 30,571,113-30,571,113 , GRCh37 chr9: 30,707,341-30,707,341 , GRCh37 chr9: 37,701,782-37,701,782 , GRCh37 chr9: 38,487,439-38,487,439 , GRCh37 chr2: 167,032,590-167,032,590 , GRCh37 chr2: 167,842,497-167,842,497 , GRCh37 chr2: 167,842,499-167,842,499 , GRCh37 chr2: 174,340,639-174,340,639 , GRCh37 chr2: 174,445,538-174,445,538 , GRCh37 chr2: 174,873,088-174,873,088 , GRCh37 chr2: 174,894,149-174,894,149 , GRCh37 chr2: 174,894,154-174,894,154 , GRCh37 chr2: 175,139,578-175,139,578 , GRCh37 chr2: 175,197,757-175,197,757 , GRCh37 chr2: 176,857,275-176,857,275 , GRCh37 chr2: 180,681,360-180,681,360 , GRCh37 chr2: 181,414,519-181,414,519 , GRCh37 chr8: 58,550,183-58,550,183 , GRCh37 chr9: 13,643,427-13,643,427 , GRCh37 chr9: 32,809,746-32,809,746 , GRCh37 chr9: 32,809,747-32,809,747 , GRCh37 chr9: 37,701,782-37,701,782 , GRCh37 chr2: 167,032,588-167,032,588 , GRCh37 chr2: 167,032,703-167,032,703 , GRCh37 chr2: 174,582,948-174,582,948 , GRCh37 chr2: 175,197,735-175,197,735 , GRCh37 chr2: 176,751,444-176,751,444 , GRCh37 chr2: 176,751,445-176,751,445 , GRCh37 chr2: 176,857,274-176,857,274 , GRCh37 chr2: 180,737,222-180,737,222 , GRCh37 chr2: 167,404,982-167,404,982 , GRCh37 chr2: 174,340,625-174,340,625 , GRCh37 chr2: 174,445,536-174,445,536 , GRCh37 chr2: 174,582,948-174,582,948 , GRCh37 chr2: 175,139,579-175,139,579 , GRCh37 chr2: 176,643,961-176,643,961 , GRCh37 chr2: 180,681,362-180,681,362 , GRCh37 chr8: 58,906,797-58,906,797 , GRCh37 chr8: 59,535,603-59,535,603 , GRCh37 chr9: 15,353,188-15,353,188 , GRCh37 chr9: 24,354,927-24,354,927 , GRCh37 chr9: 25,553,959-25,553,959 , GRCh37 chr2: 181,096,215-181,096,215 , GRCh37 chr2: 181,265,669-181,265,669 , GRCh37 chr2: 181,265,670-181,265,670 , GRCh37 chr7: 149,006,955-149,006,955 , GRCh37 chr8: 57,149,796-57,149,796 , GRCh37 chr8: 59,767,519-59,767,519 , GRCh37 chr8: 59,767,522-59,767,522 , GRCh37 chr9: 14,497,717-14,497,717 , GRCh37 chr9: 16,355,038-16,355,038 , GRCh37 chr9: 16,355,039-16,355,039 , GRCh37 chr9: 24,354,925-24,354,925 , GRCh37 chr9: 25,553,960-25,553,960 , GRCh37 chr9: 30,707,342-30,707,342 , GRCh37 chr9: 33,924,070-33,924,070 , GRCh37 chr9: 30,076,487-30,076,487 , GRCh37 chr9: 30,076,489-30,076,489 , GRCh37 chr9: 32,391,692-32,391,692 , GRCh37 chr9: 32,391,692-32,391,692 , GRCh37 chr9: 33,924,067-33,924,067 , GRCh37 chr9: 38,487,485-38,487,485 , GRCh38.p12 chr2: 166,176,080-166,176,080 , GRCh38.p12 chr2: 166,537,236-166,537,236 , GRCh38.p12 chr2: 166,548,472-166,548,472 , GRCh38.p12 chr2: 173,475,897-173,475,897 , GRCh38.p12 chr2: 173,475,911-173,475,911 , GRCh38.p12 chr2: 174,029,421-174,029,421 , GRCh38.p12 chr2: 175,779,221-175,779,221 , GRCh38.p12 chr2: 175,779,233-175,779,233 , GRCh38.p12 chr2: 179,816,633-179,816,633 , GRCh38.p12 chr2: 179,872,495-179,872,495 , GRCh38.p12 chr2: 180,400,942-180,400,942 , GRCh38.p12 chr2: 180,549,792-180,549,792 , GRCh38.p12 chr9: 13,643,428-13,643,428 , GRCh38.p12 chr9: 15,353,190-15,353,190 , GRCh38.p12 chr9: 15,353,190-15,353,190 , GRCh38.p12 chr9: 16,355,041-16,355,041 , GRCh38.p12 chr9: 30,076,489-30,076,489 , GRCh38.p12 chr9: 32,809,749-32,809,749 , GRCh38.p12 chr9: 33,924,072-33,924,072 , GRCh38.p12 chr9: 37,701,785-37,701,785 , GRCh38.p12 chr9: 38,487,488-38,487,488 , GRCh38.p12 chr2: 166,176,193-166,176,193 , GRCh38.p12 chr2: 166,176,193-166,176,193 , GRCh38.p12 chr2: 166,537,236-166,537,236 , GRCh38.p12 chr2: 166,548,472-166,548,472 , GRCh38.p12 chr2: 166,985,989-166,985,989 , GRCh38.p12 chr2: 173,580,808-173,580,808 , GRCh38.p12 chr2: 174,008,360-174,008,360 , GRCh38.p12 chr2: 174,029,426-174,029,426 , GRCh38.p12 chr2: 174,614,342-174,614,342 , GRCh38.p12 chr2: 175,886,716-175,886,716 , GRCh38.p12 chr2: 180,400,943-180,400,943 , GRCh38.p12 chr2: 180,549,793-180,549,793 , GRCh38.p12 chr7: 149,309,863-149,309,863 , GRCh38.p12 chr8: 57,637,624-57,637,624 , GRCh38.p12 chr8: 57,637,624-57,637,624 , GRCh38.p12 chr8: 57,994,238-57,994,238 , GRCh38.p12 chr8: 58,623,043-58,623,043 , GRCh38.p12 chr8: 58,623,044-58,623,044 , GRCh38.p12 chr9: 14,497,719-14,497,719 , GRCh38.p12 chr9: 14,497,728-14,497,728 , GRCh38.p12 chr9: 24,354,927-24,354,927 , GRCh38.p12 chr9: 30,076,491-30,076,491 , GRCh38.p12 chr9: 30,707,343-30,707,343 , GRCh38.p12 chr9: 30,707,344-30,707,344 , GRCh38.p12 chr9: 32,809,748-32,809,748 , GRCh38.p12 chr2: 166,985,987-166,985,987 , GRCh38.p12 chr2: 173,718,220-173,718,220 , GRCh38.p12 chr2: 174,008,443-174,008,443 , GRCh38.p12 chr2: 174,274,850-174,274,850 , GRCh38.p12 chr2: 174,274,851-174,274,851 , GRCh38.p12 chr2: 174,333,007-174,333,007 , GRCh38.p12 chr2: 179,872,489-179,872,489 , GRCh38.p12 chr2: 180,231,497-180,231,497 , GRCh38.p12 chr8: 58,854,960-58,854,960 , GRCh38.p12 chr8: 58,854,963-58,854,963 , GRCh38.p12 chr9: 30,570,815-30,570,815 , GRCh38.p12 chr9: 30,571,115-30,571,115 , GRCh38.p12 chr9: 32,391,694-32,391,694 , GRCh38.p12 chr9: 33,924,069-33,924,069 , GRCh38.p12 chr9: 37,701,785-37,701,785 , GRCh38.p12 chr2: 166,176,078-166,176,078 , GRCh38.p12 chr2: 173,580,810-173,580,810 , GRCh38.p12 chr2: 173,718,220-173,718,220 , GRCh38.p12 chr2: 174,333,029-174,333,029 , GRCh38.p12 chr2: 174,614,341-174,614,341 , GRCh38.p12 chr2: 175,886,717-175,886,717 , GRCh38.p12 chr2: 175,992,546-175,992,546 , GRCh38.p12 chr2: 175,992,547-175,992,547 , GRCh38.p12 chr2: 179,816,635-179,816,635 , GRCh38.p12 chr2: 180,231,488-180,231,488 , GRCh38.p12 chr7: 149,309,864-149,309,864 , GRCh38.p12 chr8: 56,237,237-56,237,237 , GRCh38.p12 chr8: 56,237,242-56,237,242 , GRCh38.p12 chr8: 57,994,231-57,994,231 , GRCh38.p12 chr9: 13,643,428-13,643,428 , GRCh38.p12 chr9: 16,355,040-16,355,040 , GRCh38.p12 chr9: 24,354,929-24,354,929 , GRCh38.p12 chr9: 25,553,961-25,553,961 , GRCh38.p12 chr9: 25,553,962-25,553,962 , GRCh38.p12 chr9: 32,391,694-32,391,694 , GRCh38.p12 chr9: 38,487,442-38,487,442 LNPK, NSMAF, 15 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center