9-0022-003 AND nstd173 - dbVar - NCBI

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Items: 19

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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
nsv4369954	copy number variation	20	nstd173	human		GRCh37 chr20: 14,781,684-14,823,472 , GRCh38.p12 chr20: 14,801,038-14,842,826	MACROD2
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
nsv4388323	copy number variation	1	nstd173	human		GRCh37 chr12: 86,971,755-87,022,575 , GRCh38.p12 chr12: 86,577,978-86,628,798	MGAT4C
nsv4374158	copy number variation	106	nstd173	human		GRCh37 chr3: 128,380,595-128,412,365 , GRCh38.p12 chr3: 128,661,752-128,693,522	POU5F1P6
nsv4383096	copy number variation	1	nstd173	human		GRCh37 chr16: 77,206,295-77,227,884 , GRCh38.p12 chr16: 77,172,398-77,193,987	MON1B
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
nsv4377431	copy number variation	3	nstd173	human		GRCh37 chr1: 9,304,745-9,399,934 , GRCh38.p12 chr1: 9,244,686-9,339,875	H6PD, SPSB1
nsv4370277	copy number variation	687	nstd173	human		GRCh37 chr5: 180,378,754-180,430,789 , GRCh38.p12 chr5: 180,951,754-181,003,789	BTNL8, ARPP19P1, 3 more genes
nsv4376452	copy number variation	337	nstd173	human		GRCh37 chr17: 34,437,494-34,477,480 , GRCh38.p12 chr17: 36,110,101-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 64,198-104,195 , GRCh38.p12 chr17\|NT_187614.1: 345,022-385,008	LOC101927369, LOC107985055, 3 more genes
nsv4369419	copy number variation	42	nstd173	human		GRCh37 chr14: 74,001,111-74,038,771 , GRCh38.p12 chr14: 73,534,407-73,572,067	ACOT2, HEATR4, 3 more genes
nsv4368821	copy number variation	1373	nstd173	human		GRCh37 chr22: 24,353,749-24,385,040 , GRCh38.p12 chr22\|NT_187633.1: 247,924-279,215	LOC391322, GSTTP2, 3 more genes
nsv4370840	copy number variation	154	nstd173	human		GRCh37 chr12: 11,222,368-11,247,388 , GRCh38.p12 chr12: 11,069,769-11,094,789	TAS2R43, TAS2R64P, 3 more genes
nsv4366832	copy number variation	4	nstd173	human		GRCh37 chr1: 248,688,587-248,828,223 , GRCh38.p12 chr1: 248,525,286-248,664,922	OR2AS1P, OR2T34, 6 more genes
nsv4366546	copy number variation	98	nstd173	human		GRCh37 chr3: 162,524,824-162,626,676 , GRCh38.p12 chr3: 162,807,036-162,908,888	0
nsv4375525	copy number variation	4	nstd173	human		GRCh37 chr14: 22,409,771-22,995,123 , GRCh38.p12 chr14: 21,941,580-22,526,154	TRA, TRAV38-1, 94 more genes
nsv4369741	copy number variation	1	nstd173	human		GRCh37 chr16: 34,466,679-34,765,444 , GRCh38.p12 chr16: 35,232,308-35,531,073	FRG2DP, LOC105371200, 26 more genes
nsv4380787	copy number variation	76	nstd173	human		GRCh37 chr7: 38,294,983-38,387,020 , GRCh38.p12 chr7: 38,255,382-38,347,419	TRG, TRGV5P, 18 more genes
nsv4367310	copy number variation	1	nstd173	human		GRCh37 chr12: 87,380,702-87,428,589 , GRCh38.p12 chr12: 86,986,925-87,034,812 , GRCh38.p12 chr12\|NW_015148967.1: 218,547-266,434	0
nsv4368473	copy number variation	289	nstd173	human		GRCh37 chr22: 42,918,351-42,943,641 , GRCh38.p12 chr22: 42,522,345-42,547,635	0

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