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 160

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7098892copy number variation1nstd102humanPathogenic GRCh37 chr15: 84,228,005-102,264,590 , GRCh38.p12 chr15: 83,559,253-101,724,387 CIB1, RPS12P26, 326 more genes
    nsv6972325copy number variation1nstd229human GRCh38 chr15: 92,562,016-92,570,458 , GRCh37.p13 chr15: 93,105,246-93,113,688 LINC00930
    nsv6965127copy number variation1nstd229human GRCh38 chr15: 92,429,903-92,578,172 , GRCh37.p13 chr15: 92,973,133-93,121,402 ST8SIA2, C15orf32, 2 more genes
    nsv6637683copy number variation1nstd102humanPathogenic GRCh37 chr15: 77,512,817-102,035,027 , GRCh38.p12 chr15: 77,220,475-101,494,824 LINC02253, LOC107984790, 463 more genes
    nsv6510007copy number variation1nstd223human GRCh38 chr15: 92,571,116-92,575,257 , GRCh37.p13 chr15: 93,114,346-93,118,487 LINC00930
    nsv6291795copy number variation1nstd102humanPathogenic GRCh37 chr15: 89,520,451-93,926,491 , GRCh38.p12 chr15: 88,977,220-93,383,262 LINC00930, TRY-GTA12-1, 106 more genes
    nsv6290316copy number variation1nstd102humanPathogenic GRCh37 chr15: 88,465,861-94,411,846 , GRCh38.p12 chr15: 87,922,630-93,868,617 LOC105370964, MRPL46, 130 more genes
    nsv6133155copy number variation1nstd213human GRCh37 chr15: 72,730,000-102,440,001 , GRCh38.p12 chr15: 72,437,659-101,899,798 , BLM, 609 more genes
    nsv6132919copy number variation1nstd213human GRCh37 chr15: 91,580,000-100,660,001 , GRCh38.p12 chr15: 91,036,770-100,119,796 ST8SIA2, SYNM, 116 more genes
    nsv6132917copy number variation1nstd213human GRCh37 chr15: 90,230,000-95,470,001 , GRCh38.p12 chr15: 89,686,769-94,926,772 BLM, ST8SIA2, 101 more genes
    nsv6112780copy number variation1nstd102humanPathogenic GRCh37 chr15: 92,335,751-102,399,741 , GRCh38.p12 chr15: 91,792,521-101,859,538 LOC105371009, ST8SIA2, 149 more genes
    nsv6096472insertion1nstd212human GRCh38 chr15: 92,571,483-92,571,483 , GRCh37.p13 chr15: 93,114,713-93,114,713 LINC00930
    nsv5935314copy number variation1nstd209human GRCh38 chr15: 92,571,415-92,571,493 , GRCh37.p13 chr15: 93,114,645-93,114,723 LINC00930
    nsv5649102insertion1nstd207human GRCh38 chr15: 92,571,382-92,571,382 , GRCh37.p13 chr15: 93,114,612-93,114,612 LINC00930
    nsv5531067copy number variation1nstd206human GRCh38 chr15: 92,402,520-97,547,707 , GRCh37.p13 chr15: 92,945,750-98,090,937 , LOC105371004, 71 more genes
    nsv5526101copy number variation1nstd206human GRCh38 chr15: 92,496,979-92,603,303 , GRCh37.p13 chr15: 93,040,209-93,146,533 LINC00930, C15orf32
    nsv5002420copy number variation1nstd200human GRCh38 chr15: 92,571,116-92,575,257 , GRCh37.p13 chr15: 93,114,346-93,118,487 LINC00930
    nsv5002419copy number variation1nstd200human GRCh38 chr15: 92,562,016-92,570,451 , GRCh37.p13 chr15: 93,105,246-93,113,681 LINC00930
    nsv4760880insertion1nstd199human GRCh37 chr15: 93,114,619-93,114,619 , GRCh38.p12 chr15: 92,571,389-92,571,389 LINC00930
    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