7-0055-003 AND nstd173 - dbVar - NCBI

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4388543	copy number variation	1	nstd173	human		GRCh37 chr2: 206,330,106-206,472,400 , GRCh38.p12 chr2: 205,465,382-205,607,676	PARD3B
nsv4379109	copy number variation	1337	nstd173	human		GRCh37 chr20: 1,560,774-1,597,997 , GRCh38.p12 chr20: 1,580,128-1,617,351	SIRPB1
nsv4375212	copy number variation	547	nstd173	human		GRCh37 chr1: 72,762,663-72,811,904 , GRCh38.p12 chr1: 72,296,980-72,346,221 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-67,446	RPL31P12, LOC105378797
nsv4366472	copy number variation	183	nstd173	human		GRCh37 chr3: 46,793,072-46,849,588 , GRCh38.p12 chr3: 46,751,582-46,808,098	PRSS44P, PRSS43P
nsv4383677	copy number variation	15	nstd173	human		GRCh37 chr14: 48,231,930-48,277,484 , GRCh38.p12 chr14: 47,762,727-47,808,281	LINC00648, LOC100420098
nsv4369926	copy number variation	1	nstd173	human		GRCh37 chr13: 60,487,796-60,730,636 , GRCh38.p12 chr13: 59,913,662-60,156,502	DIAPH3-AS2, DIAPH3, 2 more genes
nsv4384620	copy number variation	51	nstd173	human		GRCh37 chr6: 257,049-294,826 , GRCh38.p12 chr6: 257,049-294,826	DUSP22, , 1 more genes
nsv4369039	copy number variation	23	nstd173	human		GRCh37 chr14: 74,006,706-74,029,902 , GRCh38.p12 chr14: 73,540,002-73,563,198	ACOT1, NT5CP2, 1 more genes
nsv4365422	copy number variation	11	nstd173	human		GRCh37 chr4: 69,366,693-69,485,827 , GRCh38.p12 chr4: 68,500,975-68,620,109	LOC100132651, UGT2B17, 2 more genes
nsv4382082	copy number variation	609	nstd173	human		GRCh37 chr11: 55,374,019-55,442,305 , GRCh38.p12 chr11: 55,606,543-55,674,829	OR4C6, OR4P4, 2 more genes
nsv4377875	copy number variation	73	nstd173	human		GRCh37 chr5: 180,375,302-180,430,797 , GRCh38.p12 chr5: 180,948,302-181,003,797	BTNL8, BTNL3, 3 more genes
nsv4386129	copy number variation	134	nstd173	human		GRCh37 chr17: 34,439,977-34,477,480 , GRCh38.p12 chr17: 36,112,584-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 66,681-104,195 , GRCh38.p12 chr17\|NT_187614.1: 347,505-385,008	LOC101927369, LOC100419980, 2 more genes
nsv4371129	copy number variation	19	nstd173	human		GRCh37 chr12: 8,558,475-8,594,881 , GRCh38.p12 chr12: 8,405,879-8,442,285	OR7E140P, OR7E149P, 1 more genes
nsv4376806	copy number variation	247	nstd173	human		GRCh37 chr12: 11,219,930-11,247,388 , GRCh38.p12 chr12: 11,067,331-11,094,789	PRH1, PRH1-PRR4, 3 more genes
nsv4375950	copy number variation	1	nstd173	human		GRCh37 chr3: 162,521,309-162,654,716 , GRCh38.p12 chr3: 162,803,521-162,936,928	0
nsv4367492	copy number variation	84	nstd173	human		GRCh37 chr4: 161,041,291-161,080,636 , GRCh38.p12 chr4: 160,120,139-160,159,484	0
nsv4368463	copy number variation	9	nstd173	human		GRCh37 chr6: 168,333,308-168,611,331 , GRCh38.p12 chr6: 167,932,628-168,210,651	AFDN, KIF25, 6 more genes
nsv4387712	copy number variation	1	nstd173	human		GRCh37 chr14: 22,635,451-22,940,386 , GRCh38.p12 chr14: 22,167,555-22,471,396	LOC107984649, TRD, 28 more genes
nsv4368476	copy number variation	44	nstd173	human		GRCh37 chr14: 107,144,399-107,184,582 , GRCh38.p12 chr14: 106,688,382-106,776,343	IGHV2-70, IGHV1-69D, 9 more genes

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