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 560

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148112copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,489,453-18,321,582 , GRCh38.p12 chr16: 15,395,596-18,227,725 , GRCh38.p12 chr16|NT_187607.1: 1,053,559-2,659,700 MIR484, NDE1, 37 more genes
    nsv7148091copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,853,752-16,666,672 , GRCh38.p12 chr16: 14,759,895-16,572,815 RPL17P40, PKD1P3-NPIPA1, 54 more genes
    nsv7098843copy number variation1nstd102humanLikely pathogenic GRCh38 chr16: 14,683,149-16,536,956 , GRCh37.p13 chr16: 14,777,006-16,630,813 ABCC6, ABCC1, 56 more genes
    nsv7093396copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 14,927,709-16,484,731 , GRCh38.p12 chr16: 14,833,852-16,390,874 ABCC6, ABCC1, 50 more genes
    nsv7076939inversion1nstd229human GRCh38 chr16: 15,569,413-22,730,334 , GRCh37.p13 chr16: 15,663,270-22,741,655 ACSM5P1, RNU6-213P, 154 more genes
    nsv7074156inversion1nstd229human GRCh38 chr16: 15,933,179-17,256,206 , GRCh37.p13 chr16: 16,027,036-17,350,063 SPRING1P3, TCERG1P2, 20 more genes
    nsv7067918inversion1nstd229human GRCh38 chr16: 14,867,200-18,528,889 , GRCh37.p13 chr16: 14,961,057-18,540,211 NPIPA1, NDE1, 80 more genes
    nsv7065228inversion1nstd229human GRCh38 chr16: 16,206,939-18,587,719 , GRCh37.p13 chr16: 16,300,796-18,599,041 NPIPA7, LOC105371106, 42 more genes
    nsv7059035inversion1nstd229human GRCh38 chr16: 15,565,040-16,913,283 , GRCh37.p13 chr16: 15,658,897-17,007,140 PKD1P2, MIR3179-2, 25 more genes
    nsv7058379inversion1nstd229human GRCh38 chr16: 16,196,635-18,896,827 , GRCh37.p13 chr16: 16,290,492-18,908,149 LOC105376751, NOMO3, 46 more genes
    nsv6637991copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 15,316,939-18,770,833 , GRCh38.p12 chr16: 15,223,082-18,759,511 ABCC6, ABCC1, 58 more genes
    nsv6637905copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 15,509,407-16,527,476 , GRCh38.p12 chr16: 15,415,550-16,433,619 , GRCh38.p12 chr16|NT_187607.1: 1,073,529-2,094,665 ABCC6, ABCC1, 24 more genes
    nsv6637442copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 14,365,745-17,052,798 , GRCh38.p12 chr16: 14,271,888-16,958,941 ABCC6, ABCC1, 69 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    nsv6634452copy number variation1nstd102humanUncertain significance GRCh37 chr16: 15,416,716-16,529,801 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-2,096,990 , GRCh38.p12 chr16: 15,322,859-16,435,944 MIR3179-2, MPV17L, 26 more genes
    nsv6634451copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 15,458,733-18,520,588 , GRCh38.p12 chr16: 15,364,876-18,426,731 , GRCh38.p12 chr16|NT_187607.1: 1,022,822-2,659,700 ABCC6, ABCC1, 52 more genes
    nsv6634404copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 15,457,516-17,564,653 , GRCh38.p12 chr16: 15,363,659-17,470,796 , GRCh38.p12 chr16|NT_187607.1: 1,021,605-2,659,700 ABCC6, ABCC1, 34 more genes
    nsv6623559copy number variation1nstd224human GRCh37 chr16: 15,369,019-18,166,320 , GRCh38.p12 chr16: 15,275,162-18,072,463 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-2,659,700 ABCC1, MYH11, 37 more genes
    nsv6623406copy number variation1nstd224human GRCh37 chr16: 15,381,715-18,166,320 , GRCh38.p12 chr16: 15,287,858-18,072,463 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-2,659,700 ABCC6, MYH11, 37 more genes
    nsv6623375copy number variation1nstd224human GRCh37 chr16: 15,493,046-18,166,320 , GRCh38.p12 chr16: 15,399,189-18,072,463 , GRCh38.p12 chr16|NT_187607.1: 1,057,154-2,659,700 MARF1, RPL7P47, 35 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